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Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus
Recent studies demonstrate that several polyphenolic compounds produced from beyond the canonical monolignol biosynthetic pathways can behave as lignin monomers, participating in radical coupling reactions and being incorporated into lignin polymers. Here, we show various classes of flavonoids, the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774827/ https://www.ncbi.nlm.nih.gov/pubmed/34662399 http://dx.doi.org/10.1093/plphys/kiab469 |
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author | Rencoret, Jorge Rosado, Mario J Kim, Hoon Timokhin, Vitaliy I Gutiérrez, Ana Bausch, Florian Rosenau, Thomas Potthast, Antje Ralph, John del Río, José C |
author_facet | Rencoret, Jorge Rosado, Mario J Kim, Hoon Timokhin, Vitaliy I Gutiérrez, Ana Bausch, Florian Rosenau, Thomas Potthast, Antje Ralph, John del Río, José C |
author_sort | Rencoret, Jorge |
collection | PubMed |
description | Recent studies demonstrate that several polyphenolic compounds produced from beyond the canonical monolignol biosynthetic pathways can behave as lignin monomers, participating in radical coupling reactions and being incorporated into lignin polymers. Here, we show various classes of flavonoids, the chalconoid naringenin chalcone, the flavanones naringenin and dihydrotricin, and the flavone tricin, incorporated into the lignin polymer of papyrus (Cyperus papyrus L.) rind. These flavonoids were released from the rind lignin by Derivatization Followed by Reductive Cleavage (DFRC), a chemical degradative method that cleaves the β-ether linkages, indicating that at least a fraction of each was integrated into the lignin as β-ether-linked structures. Due to the particular structure of tricin and dihydrotricin, whose C-3ʹ and C-5ʹ positions at their B-rings are occupied by methoxy groups, these compounds can only be incorporated into the lignin through 4ʹ–O–β bonds. However, naringenin chalcone and naringenin have no substituents at these positions and can therefore form additional carbon–carbon linkages, including 3ʹ– or 5ʹ–β linkages that form phenylcoumaran structures not susceptible to cleavage by DFRC. Furthermore, Nuclear Magnetic Resonance analysis indicated that naringenin chalcone can also form additional linkages through its conjugated double bond. The discovery expands the range of flavonoids incorporated into natural lignins, further broadens the traditional definition of lignin, and enhances the premise that any phenolic compound present at the cell wall during lignification could be oxidized and potentially integrated into the lignin structure, depending only on its chemical compatibility. This study indicates that papyrus lignin has a unique structure, as it is the only lignin known to date that integrates such a diversity of phenolic compounds from different classes of flavonoids. This discovery will open up new ways to engineer and design lignins with specific properties and for enhanced value. |
format | Online Article Text |
id | pubmed-8774827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87748272022-01-21 Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus Rencoret, Jorge Rosado, Mario J Kim, Hoon Timokhin, Vitaliy I Gutiérrez, Ana Bausch, Florian Rosenau, Thomas Potthast, Antje Ralph, John del Río, José C Plant Physiol Research Articles Recent studies demonstrate that several polyphenolic compounds produced from beyond the canonical monolignol biosynthetic pathways can behave as lignin monomers, participating in radical coupling reactions and being incorporated into lignin polymers. Here, we show various classes of flavonoids, the chalconoid naringenin chalcone, the flavanones naringenin and dihydrotricin, and the flavone tricin, incorporated into the lignin polymer of papyrus (Cyperus papyrus L.) rind. These flavonoids were released from the rind lignin by Derivatization Followed by Reductive Cleavage (DFRC), a chemical degradative method that cleaves the β-ether linkages, indicating that at least a fraction of each was integrated into the lignin as β-ether-linked structures. Due to the particular structure of tricin and dihydrotricin, whose C-3ʹ and C-5ʹ positions at their B-rings are occupied by methoxy groups, these compounds can only be incorporated into the lignin through 4ʹ–O–β bonds. However, naringenin chalcone and naringenin have no substituents at these positions and can therefore form additional carbon–carbon linkages, including 3ʹ– or 5ʹ–β linkages that form phenylcoumaran structures not susceptible to cleavage by DFRC. Furthermore, Nuclear Magnetic Resonance analysis indicated that naringenin chalcone can also form additional linkages through its conjugated double bond. The discovery expands the range of flavonoids incorporated into natural lignins, further broadens the traditional definition of lignin, and enhances the premise that any phenolic compound present at the cell wall during lignification could be oxidized and potentially integrated into the lignin structure, depending only on its chemical compatibility. This study indicates that papyrus lignin has a unique structure, as it is the only lignin known to date that integrates such a diversity of phenolic compounds from different classes of flavonoids. This discovery will open up new ways to engineer and design lignins with specific properties and for enhanced value. Oxford University Press 2021-10-18 /pmc/articles/PMC8774827/ /pubmed/34662399 http://dx.doi.org/10.1093/plphys/kiab469 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Articles Rencoret, Jorge Rosado, Mario J Kim, Hoon Timokhin, Vitaliy I Gutiérrez, Ana Bausch, Florian Rosenau, Thomas Potthast, Antje Ralph, John del Río, José C Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title | Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title_full | Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title_fullStr | Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title_full_unstemmed | Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title_short | Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
title_sort | flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774827/ https://www.ncbi.nlm.nih.gov/pubmed/34662399 http://dx.doi.org/10.1093/plphys/kiab469 |
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